KEURIG DR PEPPER Recall: Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error. - F-0361-2022

🇺🇸 United States

1. December 9, 2021 - Recall initiated
2. January 12, 2022 - Reported by source
3. June 16, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0361-2022

Event ID

89191

Status

Terminated

Classification

Class II

Company

KEURIG DR PEPPER

Product description

Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Expiration Date: February 5, 2022. UPC single bottles: 0 7618300314 5. UPC 12 Pack 0 7618300813 3.

Quantity

11,970 cases

Reason

Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.

Recall initiation date

December 9, 2021

Report date

January 12, 2022

Classification date

Not published in this source record

Termination date

June 16, 2022

Distribution pattern

Distributed to 11 warehouses who then further distributed product to retailer, institutions, businesses, etc. throughout the US.

UPC, lot, and code information

ALN 09H21 (Time Stamp 18:22-23:59) and ALN 10H21 (Time Stamp 00:00-00:25)

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: KEURIG DR PEPPER

Other recalls from KEURIG DR PEPPER

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of June 16, 2022.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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